A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437518



Internal ID21095071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37213129..37213447hg38UCSC Ensembl
chr9:37213126..37213444hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187726
Samples
Known GenesZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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